Helonias Combination Liquid
NDC Package 63083-9227-1
Package Information
Helonias Combination liquids is for the temporary relief of mild to moderate pain, inflammation, nausea, or occasional headache associated with dysmenorrhea.*. This formulation utilizes a liquid delivery system. Marketed by Professional Complementary Health Formulas, this product is identified by NDC 63083-9227.
Identification & Billing
Clinical Specifications
- AMMONIUM BROMIDE 8 [hp_X]/29.5mL
- APIS MELLIFERA 4 [hp_X]/29.5mL
- BLACK COHOSH 4 [hp_X]/29.5mL
- CHAMAELIRIUM LUTEUM ROOT 6 [hp_X]/29.5mL
- CHLAMYDIA TRACHOMATIS 12 [hp_X]/29.5mL
- GOLD MONOIODIDE 12 [hp_X]/29.5mL
- LACHESIS MUTA VENOM 12 [hp_X]/29.5mL
- LILIUM LANCIFOLIUM WHOLE FLOWERING 4 [hp_X]/29.5mL
- LYCOPODIUM CLAVATUM SPORE 4 [hp_X]/29.5mL
- MELILOTUS OFFICINALIS TOP 4 [hp_X]/29.5mL
- MERCURIC CHLORIDE 12 [hp_X]/29.5mL
- NAJA NAJA VENOM 12 [hp_X]/29.5mL
- PALLADIUM 12 [hp_X]/29.5mL
- PULSATILLA MONTANA WHOLE 4 [hp_X]/29.5mL
- VESPA CRABRO 4 [hp_X]/29.5mL
- VIBURNUM OPULUS BARK 2 [hp_X]/29.5mL
Regulatory & Marketing
Hierarchy Structure
- 63083 - Professional Complementary Health Formulas
- 63083-9227 - Helonias Combination
- 63083-9227-1 - 29.5 mL in 1 BOTTLE, DROPPER
- 63083-9227 - Helonias Combination
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 63083-9227-1 identifies a specific commercial package of 29.5 ml in 1 bottle, dropper of Helonias Combination 9227, a human over the counter drug labeled by Professional Complementary Health Formulas. This liquid is formulated for oral use and contains ammonium bromide; apis mellifera; black cohosh; chamaelirium luteum root; chlamydia trachomatis; gold monoiodide; lachesis muta venom; lilium lancifolium whole flowering; lycopodium clavatum spore; melilotus officinalis top; mercuric chloride; naja naja venom; palladium; pulsatilla montana whole; vespa crabro; viburnum opulus bark as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Professional Complementary Health Formulas on August 15, 1984. The current certification is valid through December 31, 2027.
How is this Professional Complementary Health Formulas product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 63083922701. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.